Canonical Allele Identifier: CA1286883395

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426090T= , CM000664.2:g.127426090T=	GRCh38
NC_000002.11:g.128183666T= , CM000664.1:g.128183666T=	GRCh37
NC_000002.10:g.127900136T=	NCBI36
NG_016323.1:g.12671T= , LRG_599:g.12671T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.541T= MANE Select	ENSP00000234071.4:p.Phe181=
ENST00000234071.7:c.541T=	ENSP00000234071.3:p.Phe181=
ENST00000402125.2:c.121-2267T=
ENST00000409048.1:c.643T=	ENSP00000386679.1:p.Phe215=
ENST00000442644.5:c.484T=	ENSP00000411241.1:p.Phe162=
ENST00000464089.1:n.127T=
NM_000312.3:c.541T= , LRG_599t1:c.541T=	NP_000303.1:p.Phe181=
XM_005263715.3:c.724T=	XP_005263772.1:p.Phe242=
XM_005263716.3:c.706T=	XP_005263773.1:p.Phe236=
XM_005263717.3:c.604T=	XP_005263774.1:p.Phe202=
XM_005263717.4:c.604T=	XP_005263774.1:p.Phe202=
XM_017004505.1:c.784T=	XP_016859994.1:p.Phe262=
XM_024453002.1:c.886T=	XP_024308770.1:p.Phe296=
XM_024453003.1:c.826T=	XP_024308771.1:p.Phe276=
XM_024453004.1:c.724T=	XP_024308772.1:p.Phe242=
XM_024453005.1:c.706T=	XP_024308773.1:p.Phe236=
XM_024453006.1:c.643T=	XP_024308774.1:p.Phe215=
XR_923313.2:n.4495A=
NM_000312.4:c.541T= MANE Select	NP_000303.1:p.Phe181=
NM_001375602.1:c.724T=	NP_001362531.1:p.Phe242=
NM_001375603.1:c.706T=	NP_001362532.1:p.Phe236=
NM_001375604.1:c.604T=	NP_001362533.1:p.Phe202=
NM_001375605.1:c.643T=	NP_001362534.1:p.Phe215=
NM_001375606.1:c.709T=	NP_001362535.1:p.Phe237=
NM_001375607.1:c.727T=	NP_001362536.1:p.Phe243=
NM_001375608.1:c.484T=	NP_001362537.1:p.Phe162=
NM_001375609.1:c.517T=	NP_001362538.1:p.Phe173=
NM_001375610.1:c.535T=	NP_001362539.1:p.Phe179=
NM_001375611.1:c.541T=	NP_001362540.1:p.Phe181=
NM_001375613.1:c.541T=	NP_001362542.1:p.Phe181=